Current and Emerging Treatment Options in Pediatric Onset Multiple Sclerosis

Author:

Mavridi Artemis1ORCID,Bompou Maria Eleni1,Redmond Aine2,Archontakis-Barakakis Paraschos3,Vavougios George D.4ORCID,Mitsikostas Dimos D.5,Mavridis Theodoros25ORCID

Affiliation:

1. First Department of Pediatrics, School of Medicine, “Aghia Sofia” Children’s Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece

2. Department of Neurology, Tallaght University Hospital (TUH), D24 NR0A Dublin, Ireland

3. Redington-Fairview General Hospital, Skowhegan, ME 04976, USA

4. Department of Neurology, Medical School, University of Cyprus, Nicosia 1678, Cyprus

5. 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, 11528 Athens, Greece

Abstract

Pediatric onset multiple sclerosis (POMS), characterized by the onset of multiple sclerosis before the age of 18, is gaining increased recognition. Approximately 5 percent of MS cases manifest before the age of 18, with less than 1 percent occurring before the age of 10. Despite its rarity, pediatric MS exhibits distinct characteristics, with an association between younger age at onset and a comparatively slower disease progression. Despite this slower progression, individuals with POMS historically reach disability milestones at earlier ages than those with adult-onset multiple sclerosis. While various immunomodulatory agents demonstrate significant benefits in MS treatment, such as reduced relapse rates and slower accumulation of brain lesions on magnetic resonance imaging (MRI), the majority of disease-modifying therapies (DMTs) commonly used in adult MS lack evaluation through pediatric clinical trials. Current evidence is predominantly derived from observational studies. This comprehensive review aims to consolidate existing knowledge on the mechanisms of action, efficacy, safety profiles, and recommended dosages of available DMTs specifically in the context of pediatric MS. Furthermore, this review outlines recent advancements and explores potential medications still in developmental stages, providing a thorough overview of the current landscape and future prospects for treating POMS.

Publisher

MDPI AG

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